Covalent Laboratories Private Limited, an ISO 9001:2008 & ISO 14001(2004) accreditated pharmaceutical company and WHO GMP certified for all its products, is specialized in the manufacturing of Cephalosporins. It has a wide range of products and is fast expanding to meet the present and future market demands for the high value, low volume drugs. Covalent Laboratories manufactures the Active Pharmaceutical Ingredient (API) in bulk quantities for both domestic and international markets. All the drugs manufactured me -ets USP / BP / JP standards.
Chemist / Senior Chemist Quality Control
Job description:
- Responsible for testing of all In process, Raw material, Intermediate, stability samples , cleaning samples and Finished products analysis of HPLC/UPLC/GC as per Standard testing procedure.
- Experience: 1-6 yrs
Chemist R & D/ Senior Chemist- R & D
Job description:
- API CRO, HPLC / LCMS & Method development / Regular analysis
- Experience: 2-6 yrs
Executive – Regulatory Affairs
Job description:
- Preparation of LOA (Read and understanding the requirement).
Hands on experience on Drafting of response to the DMF related queries and Technical queries. Preparation of Applicant part and Restricted part DMFs (USDMF and EUDMF).
Filling of VQ’s - Experience: 5-10 yrs
Chemist for Solvent Recovery
Job description:
- Solvent Recovery Plant/ Chemical plant/ Distillation Plant. BPCR/BMR writing/ Material reconciliation writing. Fractionation column/ Vacuum system/ Molecular sieve dryer/ Glass lined reactor/ Stainless Steel Reactor/ Centrifuge. Manpower handling.
- Experience: 1-5 yrs
Chemist – Production
Job description:
- should have good exposure on GMP
- 0-4 yrs
